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Production Engineer I

Takeda

Social Circle, GAOnsitePosted 24 days ago$58,400.00 - $91,740.00
Full TimeEntry LevelManufacturing & CMCPharmaceutical
Original posting ↗

Summary

As a Production Engineer I at Takeda, you'll provide on-shift technical and engineering support to our highly automated pharmaceutical manufacturing operations in Social Circle, Georgia. You'll work alongside Manufacturing and cross-functional technical teams to rapidly troubleshoot issues, support reliable production, and help manufacturing teams meet their operational goals. This is an early-career engineering opportunity where you'll apply foundational engineering principles to real-world manufacturing challenges while developing your technical expertise across Fractionation, Albumin, and Immunoglobulin (IG) operations.

Job description

About the Role

As a Production Engineer I at Takeda, you'll provide on-shift technical and engineering support to our highly automated pharmaceutical manufacturing operations in Social Circle, Georgia. You'll work alongside Manufacturing and cross-functional technical teams to rapidly troubleshoot issues, support reliable production, and help manufacturing teams meet their operational goals. This is an early-career engineering opportunity where you'll apply foundational engineering principles to real-world manufacturing challenges while developing your technical expertise across Fractionation, Albumin, and Immunoglobulin (IG) operations.

Shift Details

6:00pm-6:30am, 2-2-3 Rotating Schedule

How You Will Contribute

  • Provide on-shift engineering and technical support to manufacturing operations, helping rapidly troubleshoot and resolve technical issues during both ramp-up and steady-state production.
  • Support manufacturing processes across IG purification, filling and packaging, Fractionation, and Albumin purification.
  • Troubleshoot and support highly automated process equipment, including vessels, filtration and chromatography systems, UF/DF, COP washers, CIP skids, filter presses, centrifuges, isolators, automatic bottle openers, and packaging lines.
  • Support DeltaV Distributed Control Systems (DCS), programmable logic controllers (PLCs), Siemens SIMATIC IT Manufacturing Execution Systems (MES), and automation hardware.
  • Support in-process testing activities involving equipment and measurements such as pH, conductivity, and titration.
  • Participate in safety and quality investigations, applying engineering principles to help identify and resolve manufacturing issues.
  • Identify and implement opportunities to improve manufacturing performance by reducing manufacturing events, user interventions, batch record alerts, cycle time, errors, and waste.
  • Perform operational assessments to help ensure appropriate processes, procedures, tools, and training are in place.
  • Investigate and resolve issues assigned through departmental issue logs while supporting Process Unit Team projects and continuous improvement initiatives.
  • Lead or support knowledge-transfer activities, coach manufacturing personnel through technical issues, develop troubleshooting guides, and share process knowledge across shifts.

What You Bring to Takeda

  • A Bachelor's degree in Engineering is required; related engineering or technical experience is preferred.
  • Related work experience in a technical or GMP-regulated environment is preferred.
  • Foundational knowledge of engineering principles across relevant disciplines is required.
  • The ability to apply engineering concepts to troubleshoot and resolve routine technical and manufacturing problems with minimal assistance is required.
  • Strong verbal and written communication skills, including the ability to clearly discuss technical issues, are required.
  • The ability to work effectively as a collaborative member of a cross-functional manufacturing team is required.
  • The ability to work independently, take initiative, and operate with minimal supervision is required.
  • Exposure to Lean Manufacturing and Six Sigma quality techniques is preferred.
  • The ability to learn and work with manufacturing systems and automated equipment, including DeltaV, PLCs, Siemens SIMATIC IT, and automation hardware, is preferred.
  • Experience or familiarity with pharmaceutical manufacturing processes and GMP requirements is preferred.
  • The ability to adapt to a 24/7 manufacturing environment, including extended or nontraditional work schedules, is required.

Important Considerations

At Takeda, our patients rely on us to deliver quality products. As a result, we follow strict requirements in our manufacturing facilities to protect product quality, employee safety, and regulatory compliance. In this role, you may:

  • Work 12-hour shifts, including nights, weekends, and holidays, in support of a 24/7 manufacturing operation.
  • Work in a cleanroom environment and follow applicable gowning and facility requirements.
  • Wear required personal protective equipment (PPE), which may include hard hats, safety shoes, safety glasses, and hearing protection depending on the work area.
  • Work in a highly automated manufacturing environment where technical issues may require timely response and coordination across multiple functions.
  • Travel on an infrequent basis, generally less than 5%.

Requirements

  • Bachelor's degree in Engineering
  • Foundational knowledge of engineering principles
  • Ability to apply engineering concepts to troubleshoot and resolve routine technical and manufacturing problems with minimal assistance
  • Strong verbal and written communication skills
  • Ability to work effectively as a collaborative member of a cross-functional manufacturing team
  • Ability to work independently, take initiative, and operate with minimal supervision
  • Ability to adapt to a 24/7 manufacturing environment, including extended or nontraditional work schedules
  • Related work experience in a technical or GMP-regulated environment (preferred)
  • Exposure to Lean Manufacturing and Six Sigma quality techniques (preferred)
  • Ability to learn and work with manufacturing systems and automated equipment, including DeltaV, PLCs, Siemens SIMATIC IT, and automation hardware (preferred)
  • Experience or familiarity with pharmaceutical manufacturing processes and GMP requirements (preferred)

Benefits

  • Medical, Dental & Vision
  • 401(k) Matching
  • Paid Time Off

Company overview

Takeda Pharmaceutical Company Limited is a Japanese multinational pharmaceutical company founded in 1781 and incorporated in 1925. As one of the world's top 20 largest pharmaceutical companies by revenue and the third largest in Asia, Takeda specializes in developing and commercializing innovative medicines across several therapeutic areas including oncology, rare diseases, neuroscience, gastroenterology, plasma-derived therapies, and vaccines. With approximately 49,095 employees globally, the company operates research and development centers, manufacturing facilities, and commercial operations across 39 U.S. states and numerous countries worldwide. Takeda maintains dual headquarters in Tokyo and Osaka, Japan, with significant operations in Cambridge, Massachusetts, where it serves as the largest life sciences employer in the state. The company's patient-focused approach is guided by its Takeda-ism values of Integrity, Fairness, Honesty, and Perseverance, emphasizing a commitment to delivering life-transforming treatments while advancing sustainable healthcare solutions. Takeda's extensive portfolio includes both innovative biologics and small molecule drugs, supported by strategic acquisitions and partnerships that have expanded its capabilities in areas such as immuno-oncology and rare disease treatments.

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